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2000
Volume 5, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A facile synthetic approach to 3'-substituted-5-cyclopropanespirohydantoins has been developed and used to synthesize some new spirohydantoins. The key aspect is the preparation of α-carboethoxy isocyanate basing on Curtius rearrangement, which can be ring-closed to the expected spirohydantoins after the reaction with various amines and hydrazines. Interestingly the cyclopropane ring doesn't open during the whole process.

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/content/journals/loc/10.2174/157017808785740471
2008-09-01
2025-09-06
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